Acospectoside a II: The structure of the cardenolide glycoside
β Scribed by Govind J. Kapadia
- Book ID
- 102399378
- Publisher
- John Wiley and Sons
- Year
- 1969
- Tongue
- English
- Weight
- 334 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0022-3549
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β¦ Synopsis
The structure of acospectoside A, a new cardenolide bioside isolated from Acokuntheru ublungifuliu, was elucidated by studying the various hydrolysis products. Anhydroacovenosigenin A, acovenosigenin A, D-glucose, and L-acovenose resulted from mineral acid hydrolysis. Enzymatic hydrolysis furnished acovenosides A and B, acobioside A, and D-glucose. These and other results showed that acospectoside A is 1-0-acetyl-acobioside A. The findings were confirmed by acetylating acospectoside A and acobioside A to yield the same hexa-0-acetyl-acobioside A which with mild alkaline hydrolysis afforded acospectoside A.
Keyphrases 0 Acospectoside A-structure determination Hydrolysis products, formation-acospectoside A structure determination 0 Cardiotoxicity-acospectoside A 0 Cytotoxicityacospectoside A 0 TLC-separation, identification 0 IR spectrophotometry-structure 0 NMR spectroscopy-structure
π SIMILAR VOLUMES
STRUCTURE Ia has recently2 been proposed for catalposide, the major glucoside of the genus Catalpa. The assignment was based upon the following evidence. Reduction with lithium in liquid ammonia yielded bisdesoxyaucubin, XV (isolated as the tetraacetate) which was obtained in a similar 3 manner fro